Sr. Associate I, Regulatory Affairs Strategy
Skills
About This Role
Overview
- At Alcon, we are driven by the meaningful work we do to help people see brilliantly.
- We innovate boldly, champion progress, and act with speed as the global leader in eye care.
- Here, you’ll be recognized for your commitment and contributions and see your career like never before.
- Together, we go above and beyond to make an impact in the lives of our patients and customers.
- We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
- As a **Senior Associate Regulatory Affairs** supporting the EMEA Regulatory Operations team, you will be trusted to work on regulatory compliance, dossier development, and product registration activities across a diverse portfolio in Riyadh.
- Please note that for this position Saudi nationals are preferred.
- In this role, a typical day will include:
- Collaborating with regional affiliates and cross-functional teams to address regulatory requirements and health authority inquiries across the Middle East and EMEA region
- Preparing and managing regulatory dossiers, submissions, licensing activities, and labeling documentation for pharmaceuticals, medical devices, cosmetics, and food supplements
- Maintaining accurate and up-to-date submission databases, ensuring timely approvals and compliance tracking
- Supporting clinical trial disclosure and submission publishing activities with high attention to quality and regulatory standards
- Ensuring full adherence to GxP requirements, SOPs, and documentation standards to maintain audit readiness and regulatory compliance
What You’Ll Bring To Alcon
- Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, or a related field
- Minimum 3 years of experience in Regulatory Affairs within the Middle East region in a multinational medical or pharmaceutical company
- Strong knowledge of regulatory frameworks in the Middle East; understanding of EU regulations is highly desirable
- Proven ability to manage regulatory submissions, dossier preparation, and compliance documentation
- Excellent collaboration, communication, and influencing skills within matrix organizations
- Fluency in English and Arabic (written and spoken)
- High level of organization, adaptability, and a proactive, solution-oriented mindset
How You Can Thrive At Alcon
- Work in a dynamic, international environment with exposure to diverse product categories and regulatory landscapes
- Take ownership of meaningful projects that directly impact patient safety and product accessibility across markets
- Collaborate with a highly skilled, supportive team where innovation, continuous improvement, and personal growth are encouraged
Alcon Careers
See your impact at alcon.com/careers
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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